KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel

Mutations in HERG and KCNQ1 (or KVLQT1) genes cause the life-threatening Long QT syndrome. These genes encode K(+) channel pore-forming subunits that associate with ancillary subunits from the KCNE family to underlie the two components, I(Kr) and I(Ks), of the human cardiac delayed rectifier current...

Full beskrivning

Bibliografiska uppgifter

I publikationen:	EMBO J
Huvudupphov:	Tinel, Norbert, Diochot, Sylvie, Borsotto, Marc, Lazdunski, Michel, Barhanin, Jacques
Materialtyp:	Artigo
Språk:	Inglês
Utgiven:	Nature Publishing Group 2000
Ämnen:	Articles
Länkar:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC305874/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11101505/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/emboj/19.23.6326
Taggar:	Lägg till en tagg Inga taggar, Lägg till första taggen!